Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1160237842 1.000 0.160 7 151078668 missense variant A/G snv 8.0E-06 2
rs1298314972 1.000 0.160 7 151079887 missense variant G/A snv 7.0E-06 2
rs1568546120 1.000 0.160 19 45368993 splice acceptor variant C/A snv 2
rs1568546252 1.000 0.160 19 45369132 stop gained C/A snv 2
rs80357091 1.000 0.160 17 43104910 missense variant A/C;G snv 8.0E-06 2
rs964247601 1.000 0.160 19 45368692 stop gained C/A;T snv 1.2E-05 2
rs1194327405 1.000 0.160 X 71377774 missense variant G/A snv 1.1E-05 1
rs1312839452 1.000 0.160 19 54982237 missense variant A/G snv 4.0E-06 1
rs1340806384 1.000 0.160 19 45364442 missense variant C/T snv 4.0E-06 1
rs140522180 1.000 0.160 19 45353112 missense variant C/A;T snv 2.0E-05; 1.9E-04 1
rs200919197 1.000 0.160 16 85481 missense variant C/G;T snv 1.2E-05; 9.6E-05 1
rs746795177 1.000 0.160 19 45364121 splice acceptor variant T/C snv 1.3E-05 1.4E-05 1
rs752510317 1.000 0.160 19 45352556 missense variant G/A snv 1.2E-05 1
rs753641926 1.000 0.160 19 45353113 missense variant G/A;T snv 4.4E-05; 4.0E-06 1
rs758439420 1.000 0.160 19 45352351 missense variant C/A;T snv 8.0E-06; 1.6E-05 1
rs758748662 1.000 0.160 7 55155911 missense variant G/A snv 4.0E-06 1.4E-05 1
rs767747355 1.000 0.160 19 45364838 frameshift variant GAGT/- delins 1.2E-05 1
rs770085172
AGT
1.000 0.160 1 230710315 missense variant T/C snv 7.0E-06 1
rs771366736 1.000 0.160 7 55143380 missense variant A/G snv 8.0E-06 1.4E-05 1
rs771824813 1.000 0.160 19 45353109 missense variant C/T snv 4.0E-06 1
rs771929085 1.000 0.160 7 55155941 missense variant G/A snv 1.2E-05 1
rs772572683 1.000 0.160 19 45355676 missense variant C/T snv 4.0E-06 1
rs121913019 0.925 0.240 19 45354774 missense variant T/C;G snv 4.0E-06 3
rs1405999227 0.925 0.160 7 55156637 missense variant A/G snv 4.0E-06 3
rs1060503460
NBN
0.925 0.200 8 89955461 missense variant A/T snv 2